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Mutations in the AP1B1 gene cause a new syndrome with skin, hearing, and developmental issues.

Introducing the rat OTC gene partially corrected OTC deficiency in mice.

A new gene mutation may allow some piebaldism patients to regain skin color in white patches.

Hereditary factors cause hair loss in mice by affecting skin and hair follicle structure.

Blocking EGFR in mice causes hair loss and skin changes.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

FGF9 controls which receptors it binds to through a process where two FGF9 molecules join, and changes in FGF9 can lead to incorrect receptor activation.

Researchers created a mouse model for Cushing's syndrome to study glucocorticoid excess and potential treatments.

FOXN1 is crucial for thymus development and immune response in Xenopus laevis.

Msx2-deficient mice experience irregular hair growth and loss due to disrupted hair cycle phases.

Defective protein folding due to a mutation is key in ANE syndrome.

A gene mutation in mice causes increased mast cells and disorganized hair follicles in their skin.

FOXN1 mutations cause severe immunodeficiency, hair loss, nail issues, and thymus defects.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

External factors can cause skin cancer cells that usually don't spread to grow and form tumors in mice.

The mutant HR bmh protein affects hair follicle formation by failing to repress vitamin D receptor activity.

C-scores can help predict gain-of-function and loss-of-function mutations.

ING5 is crucial for stem cell maintenance and preventing certain cancers.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

A specific gene change in APCDD1 increases the risk of hair loss.

cDermo-1 causes dense skin, feathers, and scales in chickens.

A gene mutation causes monilethrix in a Chinese family.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Mice without certain skin proteins had abnormal skin and hair development.

A new mutation in the human glucocorticoid receptor reduces its function and causes resistance to glucocorticoids.

Two siblings have a rare hair condition caused by a new genetic variant.

A specific mutation in PA-PLA1α causes abnormal hair growth.